首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Quantification of montelukast, a selective cysteinyl leukotriene receptor (CysLT1) antagonist in human plasma by liquid chromatography-mass spectrometry: validation and its application to a human pharmacokinetic study.
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Quantification of montelukast, a selective cysteinyl leukotriene receptor (CysLT1) antagonist in human plasma by liquid chromatography-mass spectrometry: validation and its application to a human pharmacokinetic study.

机译:液相色谱-质谱法定量分析孟鲁司特,一种在人血浆中的选择性半胱氨酰白三烯受体(CysLT1)拮抗剂:验证及其在人体药代动力学研究中的应用。

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摘要

A highly sensitive, rapid assay method has been developed and validated for the estimation of montelukast (MTK) in human plasma with liquid chromatography coupled to tandem mass spectrometry with electro spray ionization in the positive-ion mode. Liquid-liquid extraction was used to extract MTK and amlodipine (internal standard, IS) from human plasma. Chromatographic separation was achieved with 10 mM ammonium acetate (pH 6.4): acetonitrile (15:85, v/v) at a flow rate of 0.50 mL/min on a Discovery HS C(18) column with a total run time of 3.5 min. The MS/MS ion transitions monitored were 586.10 --> 422.10 for MTK and 409.20 --> 238.30 for IS. Method validation and clinical sample analysis were performed as per FDA guidelines and the results met the acceptance criteria. The lower limit of quantitation achieved was 0.25 ng/mL and linearity was observed from 0.25 to 800 ng/mL. The intra-day and inter-day precisions were 5.97-8.33 and 7.09-10.13%, respectively. This novel method has been applied to a pharmacokinetic study of MTK in humans.
机译:已开发出一种高灵敏度,快速的测定方法,并已通过液相色谱与串联质谱联用电喷雾电离以正离子模式联用,在人血浆中孟鲁司特(MTK)的估算中得到了验证。液-液萃取用于从人血浆中萃取MTK和氨氯地平(内标,IS)。在Discovery HS C(18)色谱柱上,以0.50 mL / min的流速用10 mM乙酸铵(pH 6.4):乙腈(15:85,v / v)进行色谱分离,总运行时间为3.5分钟。监测到的MS / MS离子跃迁,MTK为586.10-> 422.10,IS为409.20-> 238.30。按照FDA指南进行方法验证和临床样品分析,结果符合接受标准。达到的定量下限为0.25 ng / mL,线性范围为0.25至800 ng / mL。日内和日间精度分别为5.97-8.33%和7.09-10.13%。此新方法已应用于人类MTK的药代动力学研究。

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